Download PDF – RRB PH UT23 – Pharmaceutical Jurisprudence Practice Test 2: Pharmacy Act 1948 & Allied Statutory Acts

RRB PH UT23 – Pharmaceutical Jurisprudence Practice Test 2: Pharmacy Act 1948 & Allied Statutory Acts

Q1. Under Section 3 of the Pharmacy Act 1948, how many members are elected by the UGC to the PCI?

A) One member

B) Two members

C) Six members

D) Three members

Q1. फार्मेसी अधिनियम, 1948 की धारा 3 के तहत UGC, PCI के लिए कितने सदस्य चुनता है?

A) एक सदस्य

B) दो सदस्य

C) छह सदस्य

D) तीन सदस्य

Answer: (C)

Under Section 3(c) of the Pharmacy Act 1948, the Central Council (PCI) includes one member elected by the University Grants Commission (UGC) from among the teaching staff of an Indian university or an affiliated college granting a degree or diploma in pharmacy or pharmaceutical chemistry. Six members are nominated by the Central Government, and six members are elected by the Inter-University Board (UGC).

फार्मेसी अधिनियम की धारा 3(a) के अनुसार UGC शिक्षण स्टाफ में से छह सदस्य चुनता है—फार्मेसी, फार्मास्यूटिकल केमिस्ट्री, फार्माकोलॉजी और फार्माकोग्नोसी के एक-एक शिक्षक सहित।

Q2. How many registered pharmacists are elected to a State Pharmacy Council under Section 19 of the Pharmacy Act 1948?

A) Three members

B) Five members

C) Six members

D) Seven members

Q2. फार्मेसी अधिनियम, 1948 की धारा 19 के तहत राज्य फार्मेसी परिषद में कितने पंजीकृत फार्मासिस्ट चुने जाते हैं?

A) तीन सदस्य

B) पाँच सदस्य

C) छह सदस्य

D) सात सदस्य

Answer: (C)

Under Section 19(a) of the Pharmacy Act 1948, a State Pharmacy Council consists of six members elected from amongst themselves by registered pharmacists residing in the State. Additionally, the Executive Committee of the State Council comprises the President, Vice-President, and three other elected council members.

धारा 19(a) के अनुसार राज्य के पंजीकृत फार्मासिस्ट अपने बीच से छह सदस्य चुनते हैं।

Q3. What is the commercial quantity of morphine under the NDPS Act 1985?

A) 5 grams

B) 250 grams

C) 1000 grams

D) 500 grams

Q3. NDPS अधिनियम, 1985 के तहत मॉर्फिन की वाणिज्यिक मात्रा कितनी है?

A) 5 ग्राम

B) 250 ग्राम

C) 1000 ग्राम

D) 500 ग्राम

Answer: (B)

Under the statutory notifications issued pursuant to the NDPS Act 1985, for Morphine: a quantity up to 5 grams is classified as 'small quantity', whereas a quantity equal to or exceeding 250 grams is legally classified as 'commercial quantity'. For Heroin (diacetylmorphine), small quantity is 5 grams and commercial quantity is 250 grams. Offenses involving commercial quantities carry rigorous imprisonment of 10 to 20 years and heavy statutory fines.

NDPS अधिसूचना के अनुसार मॉर्फिन की छोटी मात्रा 5 ग्राम और वाणिज्यिक मात्रा 250 ग्राम है।

Q4. Which authority fixes ceiling prices of scheduled formulations under DPCO 2013?

A) Central Drugs Standard Control Organization (CDSCO)

B) Pharmacy Council of India (PCI)

C) Indian Council of Medical Research (ICMR)

D) National Pharmaceutical Pricing Authority (NPPA)

Q4. DPCO 2013 के तहत अनुसूचित फॉर्मूलेशन की सीलिंग कीमत कौन तय करता है?

A) केंद्रीय औषधि मानक नियंत्रण संगठन (CDSCO)

B) फार्मेसी परिषद भारत (PCI)

C) भारतीय चिकित्सा अनुसंधान परिषद (ICMR)

D) राष्ट्रीय औषधि मूल्य निर्धारण प्राधिकरण (NPPA)

Answer: (D)

The National Pharmaceutical Pricing Authority (NPPA), an attached office of the Department of Pharmaceuticals under the Ministry of Chemicals and Fertilizers, is the independent statutory regulator tasked with monitoring pharmaceutical prices, enforcing the Drugs (Prices Control) Order (DPCO 2013), and fixing the ceiling prices of essential medicines listed in the National List of Essential Medicines (NLEM).

NPPA, औषध विभाग के अंतर्गत, DPCO लागू करता है और अनुसूचित दवाओं की सीलिंग कीमत तय करता है।

Q5. Which advertisement is prohibited under the Drugs and Magic Remedies Act 1954?

A) An advertisement promoting the hygiene benefits of medicated hand wash

B) An advertisement claiming a formulation provides a permanent cure for diabetes mellitus

C) An advertisement informing physicians about the pharmacokinetic profile of a new beta-blocker

D) An advertisement for an over-the-counter multivitamin syrup

Q5. ड्रग्स एंड मैजिक रेमेडीज अधिनियम, 1954 के तहत कौन-सा विज्ञापन प्रतिबंधित है?

A) औषधीय हैंडवॉश के स्वच्छता लाभ का विज्ञापन

B) मधुमेह के स्थायी इलाज का दावा करने वाला विज्ञापन

C) नई बीटा-ब्लॉकर की फार्माकोकाइनेटिक जानकारी चिकित्सकों को देना

D) OTC मल्टीविटामिन सिरप का विज्ञापन

Answer: (B)

Under Section 3 of the Drugs and Magic Remedies (Objectionable Advertisements) Act 1954, no person shall take part in the publication of any advertisement referring to any drug claiming procurement of miscarriage/conception in women, maintenance or improvement of sexual pleasure, correction of menstrual disorders, or diagnosis, cure, mitigation, treatment, or prevention of any disease or condition specified in the Schedule (such as Diabetes, Cancer, Epilepsy, and Blindness).

धारा 3 अनुसूची में दिए रोगों—जैसे मधुमेह, कैंसर, मिर्गी—के निदान/इलाज/रोकथाम का दावा करने वाले विज्ञापनों को प्रतिबंधित करती है।

Q6. What is the minimum D.Pharm practical training required under the PCI Education Regulations?

A) 500 hours spread over not less than 3 months

B) 250 hours spread over not less than 1 month

C) 750 hours spread over not less than 6 months

D) 1000 hours spread over not less than 12 months

Q6. PCI शिक्षा विनियमों (Education Regulations) के तहत D.Pharm का न्यूनतम व्यावहारिक प्रशिक्षण (practical training) कितना होना चाहिए?

A) कम-से-कम 3 महीने में 500 घंटे

B) कम-से-कम 1 महीने में 250 घंटे

C) कम-से-कम 6 महीने में 750 घंटे

D) कम-से-कम 12 महीने में 1000 घंटे

Answer: (A)

Under the Education Regulations (ER) prescribed by the Pharmacy Council of India pursuant to Section 10 of the Pharmacy Act 1948, every student undergoing the Diploma in Pharmacy course must complete not less than 500 hours of practical hospital or dispensary training spread over a period of not less than 3 months, of which not less than 250 hours must be devoted to actual dispensing of prescriptions.

PCI Education Regulations के अनुसार कम-से-कम 500 घंटे का प्रशिक्षण, न्यूनतम 3 महीने में; इसमें कम-से-कम 250 घंटे वास्तविक प्रिस्क्रिप्शन डिस्पेंसिंग शामिल है।

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